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Associations between antidiabetic medications and cerebrospinal fluid biomarkers of Alzheimer's disease

医学 糖尿病 二甲双胍 内科学 优势比 生物标志物 病态的 脑脊液 疾病 胰岛素 队列 逻辑回归 胃肠病学 内分泌学 生物化学 化学
作者
Gemma García‐Lluch,Anna Marseglia,Lucrecia Moreno,Juan Pardo,Mar García-Zamora,Miquel Baquero,Carmen Peña‐Bautista,Lourdes Rojas Álva­rez,Eric Westman,Consuelo Cháfer‐Pericás
出处
期刊:Journal of Alzheimer's Disease [IOS Press]
被引量:1
标识
DOI:10.1177/13872877241304995
摘要

Background It has been hypothesized that insulin resistance is pivotal in mediating amyloid and tau dysregulations in Alzheimer's disease (AD). Objective To investigate the impact of different antidiabetic agents, their daily dosage intake, and treatment duration on cerebrospinal fluid (CSF) AD biomarkers among patients with type 2 diabetes. Methods This cross-sectional study selected patients between 50 and 80 years with diabetes and CSF AD biomarkers screened between 2017 and 2023 in the VALCODIS Cohort. CSF biomarkers were total tau (t-tau), phosphorylated tau 181 (p-tau), and amyloid-β 42 (Aβ 42 ). Analytical variables were obtained. Antidiabetic prescriptions were recorded in defined daily doses (DDD), according to the ATC/DDD 2021 system, and years of drug exposure duration before lumbar puncture. Logistic regressions were performed to establish the correlations between drug usage and AD biomarker alteration. Results Among patients with diabetes, Insulin consumption was associated with lower odds of abnormal Aβ 42 levels (OR 0.36 [95% CI 0.15, 0.76]) and tau pathology (OR 0.49 [95% CI 0.24–0.98]). Metformin was related to lower odds of pathological p-tau when diabetes was uncontrolled, acting on t-tau and t-tau/Aβ 42 ratio when it was concomitant with insulin, and patients had controlled diabetes. Lower odds of pathological levels of tau were observed when additional oral antidiabetic drugs were added among metformin users. iSGLT2 was associated with tau pathology. Conclusions The impact of antidiabetics on AD-related pathological biomarkers may depend on diabetes management.
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